Formalin-fixed paraffin-embedded renal biopsy tissues: an underexploited biospecimen resource for gene expression profiling in IgA nephropathy

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作者
Sharon Natasha Cox
Samantha Chiurlia
Chiara Divella
Michele Rossini
Grazia Serino
Mario Bonomini
Vittorio Sirolli
Francesca B. Aiello
Gianluigi Zaza
Isabella Squarzoni
Concetta Gangemi
Maria Stangou
Aikaterini Papagianni
Mark Haas
Francesco Paolo Schena
机构
[1] Schena Foundation,Division of Nephrology, Dialysis, and Transplantation, Department of Emergency and Organ Transplantation
[2] Research Center of Kidney Diseases,Department of Medicine and Aging Sciences
[3] University of Bari,Renal Unit, Department of Medicine
[4] National Institute of Gastroenterology “S. de Bellis”,Department of Nephrology, Hippokration General Hospital
[5] Research Hospital,Department of Pathology and Laboratory Medicine
[6] University “G. D’Annunzio” of Chieti-Pescara,undefined
[7] University-Hospital of Verona,undefined
[8] Aristotle University of Thessaloniki,undefined
[9] Cedars-Sinai Medical Center,undefined
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Scientific Reports | / 10卷
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摘要
Primary IgA nephropathy (IgAN) diagnosis is based on IgA-dominant glomerular deposits and histological scoring is done on formalin-fixed paraffin embedded tissue (FFPE) sections using the Oxford classification. Our aim was to use this underexploited resource to extract RNA and identify genes that characterize active (endocapillary–extracapillary proliferations) and chronic (tubulo-interstitial) renal lesions in total renal cortex. RNA was extracted from archival FFPE renal biopsies of 52 IgAN patients, 22 non-IgAN and normal renal tissue of 7 kidney living donors (KLD) as controls. Genome-wide gene expression profiles were obtained and biomarker identification was carried out comparing gene expression signatures a subset of IgAN patients with active (N = 8), and chronic (N = 12) renal lesions versus non-IgAN and KLD. Bioinformatic analysis identified transcripts for active (DEFA4,TNFAIP6,FAR2) and chronic (LTB,CXCL6, ITGAX) renal lesions that were validated by RT-PCR and IHC. Finally, two of them (TNFAIP6 for active and CXCL6 for chronic) were confirmed in the urine of an independent cohort of IgAN patients compared with non-IgAN patients and controls. We have integrated transcriptomics with histomorphological scores, identified specific gene expression changes using the invaluable repository of archival renal biopsies and discovered two urinary biomarkers that may be used for specific clinical decision making.
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